CN1164558C - Method for preparing methyl phenyl oxalate and phenostal - Google Patents
Method for preparing methyl phenyl oxalate and phenostal Download PDFInfo
- Publication number
- CN1164558C CN1164558C CNB021292132A CN02129213A CN1164558C CN 1164558 C CN1164558 C CN 1164558C CN B021292132 A CNB021292132 A CN B021292132A CN 02129213 A CN02129213 A CN 02129213A CN 1164558 C CN1164558 C CN 1164558C
- Authority
- CN
- China
- Prior art keywords
- reaction
- phenol
- oxalate
- methyl phenyl
- phenyloxalate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Abstract
The present invention discloses a method for preparing methyl-phenyl-ethanedioate and phenyloxalate. The method uses dimethyl oxalate and phenol as raw materials, the charging molar ratio of raw materials of dimethyl oxalate to phenol is 1:20 to 20:1, reaction time is from 1 to 4 hours, reaction temperature is from 170 to 190 DEG C, the reaction pressure of self-generation is from 0 to 1.0MPa, and ester exchange reaction is carried out under the condition of the existence of catalysts. The present invention is characterized in that the adopted catalysts are mordenite, HZSM-5, Hbeta or TS-1 molecular sieves, and the catalysts accounts for 1/64 to 1/16 of the total charging amount according to the weight percentage. The present invention has the advantages of mild operating condition, short reaction time, high conversion rate of the raw materials, high yield of products, easy separation of the catalysts and the reaction systems, convenient serialization generation of the whole reaction system, etc.
Description
Technical field
The present invention relates to a kind of processing method that is used to prepare the raw material of diphenyl carbonate (DPC), specifically, relate to the method for preparing methyl phenyl oxalate (MPO) and phenyloxalate (DPO), be catalyzer in particular with the molecular sieve, by dimethyl oxalate (DMO) and phenol ester permutoid reaction, prepare methyl phenyl oxalate and phenyloxalate under the heterogeneous conditions.
Background technology
With dimethyl oxalate and phenol is that feedstock production methyl phenyl oxalate and phenyloxalate are that all are the gordian technique of feedstock production diphenyl carbonate with dimethyl oxalate and phenol.The reactions steps of this gordian technique experience is as follows:
Or
With this gordian technique is that the dpc production technology of core occurred in the nineties, but development rapidly, particularly Ri Ben Ube company is devoted to the research of this respect always, and applied for many patents, as EP1013633A1, US5811573, CN1164529A, TW438765, US5834615, EP0832872A1, US5922827, EP0832910A2 etc.But in above-mentioned all patents, relating to the dimethyl oxalate is raw material prepares diphenyl carbonate synthesis by transesterify raw material, when being methyl phenyl oxalate or phenyloxalate, though used transesterification catalyst is brought in constant renewal in, variation is also perfect, can be basic metal, cadmium, zirconium, plumbous, iron, copper, zn cpds or organo-tin compound, aluminium, titanium, the organic acid compound of vanadium etc., but be the homogeneous catalyst that dissolves in reaction system, promptly the transesterification reaction that will carry out to some extent be homogeneous reaction, thereby above-mentioned all patented technologies have all used complicated separation system or equipment that catalyzer is separated with reaction.
Summary of the invention
The object of the present invention is to provide a kind of is basic raw material with dimethyl oxalate and phenol, and preparation is used to produce the raw material of diphenyl carbonate, the i.e. method of methyl phenyl oxalate and phenyloxalate.The selectivity height of the transformation efficiency of DMO and MPO, DPO not only in this procedure, and process save complex separations technology and equipment to catalyzer, and therefore, this technological process is simple.
For achieving the above object, the present invention is realized by following technical proposals, with dimethyl oxalate and phenol is raw material, at raw material raw materials components mole ratio DMO: phenol=1: 20～20: 1, reaction times is 1～4 hour, temperature of reaction is 170～190 ℃, spontaneous reaction pressure is that 0～1.0Mpa reaches under the heterogeneous catalysis condition, carry out transesterification reaction, raw material MPO or the DPO of DPC produced in preparation, it is characterized in that the catalyzer that is adopted is a mordenite, HZSM-5, H β or TS-1 molecular sieve, the weight ratio of catalyst consumption and total feed are 1/64～1/16.
The preferred TS-1 molecular sieve of above-mentioned molecular sieve catalyst, Ti content is greater than 1.0wt% in the molecular sieve.
Above-mentioned catalyst consumption by weight percentage, with the weight ratio of total feed be 1/35～1/30.
The invention has the advantages that, by adopting molecular sieve catalyst, not only conversion of raw material and product selectivity all have and adopt homogeneous catalyst significantly to improve, and have save separating technology process and equipment to the complexity of catalyzer and reaction system, have reduced production cost.
Come the present invention is further specified below by specific embodiment, but do not limit the present invention.
Embodiment
[embodiment 1]
The present invention is to be that the enforcement of feedstock production methyl phenyl oxalate and phenyloxalate processing method is investigated with dimethyl oxalate and phenol under the heterogeneous catalytic reaction condition, in 250 milliliters there-necked flask, carry out, the heating of heat collecting type induction stirring is furnished with thermometer, to show the reactive system temperature.The consumption of technical grade DMO is 0.1 mole, and the amount of chemical pure phenol is 0.5 mole, and mordenite (Si/Al=30) catalyst consumption is 1.8 grams.Add under normal pressure, stir and heat up, temperature of reaction is controlled at 180.0 ± 2 ℃, and the reaction times is 2 hours.The reaction equilibrium constant in each step of reaction (1)-(3) is all minimum, for breaking the restriction of thermodynamic(al)equilibrium, improve conversion of raw material, mouth is equipped with the reflux condensing tube of the thermostatical circulating water that feeds 70 ℃ (a little more than boiling points of methyl alcohol) in the flask, the methyl alcohol that reaction generates can constantly steam from the reaction mixture system, and collects overhead product in cold-trap.After reaction finished, the mode by suction filtration was to simple the separating of reaction mass and catalyzer, and promptly available gas-chromatography is analyzed reaction result.With the transformation efficiency of DMO, the selectivity of MPO, DPO is index, investigates reactivity worth.
The data processing of reaction result is calculated as follows:
[embodiment 2]
Catalyzer is used HZSM-5 (Si/Al=25, mol ratio) instead, under other condition and embodiment 1 identical situation, carries out transesterification reaction, investigates reaction result.
[embodiment 3]
Catalyzer is used H β (Si/Al=35, mol ratio) instead, under other condition and embodiment 1 identical situation, carries out transesterification reaction, investigates reaction result.
[embodiment 4-7]
Catalyzer is used TS-1 (Ti content is 2.5 weight %) instead, and the reaction times carried out respectively 1 hour, 2 hours, 3 hours, 4 hours, under other condition and embodiment 1 identical situation, carry out transesterification reaction, investigate reaction result, form embodiment 4, embodiment 5, embodiment 6 and embodiment 7 respectively.
Reaction result is shown in Table 1.
Table 1: embodiment 1-7 transesterification reaction result (weight percentage)
Reaction DMO selectivity, % yield, %
The embodiment catalyzer
Time, hour transformation efficiency % methyl-phenoxide MPO DPO MPO DPO
1 mordenite 2 1.4 15.2 84.8 0 1.2 0
2 H-ZSM-5 2 12.5 43.9 38.1 15.4 4.8 1.9
3 Hβ 2 54.0 31.0 53.6 12.2 29.0 6.6
4 TS-1 1 24.1 1.5 92.6 5.9 22.3 1.4
5 TS-1 2 26.5 0.8 89.2 10.0 23.6 2.7
6 TS-1 3 29.2 0.7 89.9 9.4 26.2 2.7
7 TS-1 4 30.0 0.7 87.8 11.5 26.3 3.4
From above-mentioned reaction result as can be seen, the reaction result that in the processing method of the present invention with TS-1 is transesterification catalyst is best, and from embodiment 4-7 as can be seen, though the prolongation in reaction times helps promoting the carrying out that react, improve conversion of raw material and improve the yield of product, but the space-time yield of device purpose product the reaction times be 2 hours better, so consider that from the device economic performance be chosen as 2 hours the duration of contact of reaction.This moment, catalyzer had active preferably and high purpose selectivity of product, and the purpose product selectivity can reach 99.2%, and the selectivity of by product only has 0.8%, and forms simply, is mainly methyl-phenoxide.
[Comparative Examples 1-4]
Adopt Zn (OAc) respectively
2, Ti (OC
4H
9)
4, SnOBu
2Make transesterification catalyst with dibutyl tin laurate, the loadings of catalyzer is 0.01mol, in identical reaction unit, under identical operations and the feed conditions, carries out the homogeneous phase transesterification reaction.The reaction result of Comparative Examples is as shown in table 2.
Table 2: Comparative Examples transesterification reaction result
The DMO selectivity, % yield, %
The Comparative Examples catalyzer
Transformation efficiency % by product MPO DPO MPO DPO
1 Zn(OAc)
2 28.1 43.5 53.9 2.6 16.4 0.1
2 Ti(OC
4H
9)
4 92.5 76.6 20.6 2.8 19.0 2.6
3 SnOBu
2 25.7 6.7 80.8 12.5 20.8 3.2
4 dibutyl tin laurates 54.1 65.3 21.0 13.7 11.4 7.4
From embodiment and Comparative Examples as can be seen, be in the technology of feedstock production diphenyl carbonate with dimethyl oxalate and phenol, gordian technique wherein, be in the step of dimethyl oxalate and phenol ester exchange preparation methyl phenyl oxalate and phenyloxalate, if adopting the TS-1 molecular sieve is catalyzer, the purpose product selectivity exceeds the selectivity in the Comparative Examples far away, and its activity is also higher, thereby higher purpose product yield is arranged.And if with traditional transesterification catalyst, as be widely used as organic zinc, organic titanium and the organic tin compound as catalyst of transesterification catalyst, from Comparative Examples 1～4 as can be seen, except that Dibutyltin oxide, the purpose selectivity of product of other catalyzer is all extremely low; And Dibutyltin oxide is when making catalyzer, and except that costing an arm and a leg, Dibutyltin oxide decomposes voluntarily and forms homogeneous phase with system, outside catalyzer can not reclaim, also needs complicated separation system and equipment.
To sum up, with the TS-1 molecular sieve is the transesterification reaction of passing through dimethyl oxalate and phenol of feature as transesterification catalyst, synthetic methyl phenyl oxalate and the phenyloxalate that is used to prepare diphenyl carbonate, for by being raw material with dimethyl oxalate and phenol, elder generation's synthesis of methyl phenyl barkite and phenyloxalate, by further preparing diphenyl carbonate, provide more favourable key core technology then with phenol ester exchange and/or direct de-carbonyl reaction.
The invention is not restricted to above embodiment, present patent application personnel can make various changes and distortion according to the present invention, only otherwise break away from spirit of the present invention, all should belong to scope of the present invention.
Claims (3)
1. method for preparing methyl phenyl oxalate and phenyloxalate, be to be raw material with dimethyl oxalate and phenol, at raw material raw materials components mole ratio dimethyl oxalate: phenol=1: 20～20: 1, reaction times is 1～4 hour, temperature of reaction is 170～190 ℃, spontaneous reaction pressure is that 0～1.0Mpa reaches under the heterogeneous catalysis condition, carry out the process of transesterification reaction, it is characterized in that, the catalyzer that is adopted is mordenite, HZSM-5, H β or TS-1 molecular sieve, and catalyst consumption and total feed weight ratio are 1/64～1/16.
2. according to the described method for preparing methyl phenyl oxalate and phenyloxalate of claim 1, it is characterized in that the preferred TS-1 molecular sieve of molecular sieve catalyst, Ti content is greater than 1.0wt% in the molecular sieve.
3. according to the described method for preparing methyl phenyl oxalate and phenyloxalate of claim 1, the weight ratio that it is characterized in that catalyst consumption and total feed is 1/35～1/30.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021292132A CN1164558C (en) | 2002-08-28 | 2002-08-28 | Method for preparing methyl phenyl oxalate and phenostal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021292132A CN1164558C (en) | 2002-08-28 | 2002-08-28 | Method for preparing methyl phenyl oxalate and phenostal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1412176A CN1412176A (en) | 2003-04-23 |
| CN1164558C true CN1164558C (en) | 2004-09-01 |
Family
ID=4746155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB021292132A Expired - Lifetime CN1164558C (en) | 2002-08-28 | 2002-08-28 | Method for preparing methyl phenyl oxalate and phenostal |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1164558C (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103012127B (en) * | 2011-09-28 | 2015-08-26 | 中国石油化工股份有限公司 | A kind of phenol and dimethyl ester carry out the method for transesterify |
| CN103204777B (en) * | 2012-01-13 | 2014-12-31 | 中国石油化工股份有限公司 | Ester exchange catalysis method |
| CN103524341B (en) * | 2013-08-26 | 2014-12-24 | 中建安装工程有限公司 | Application of Br phi nsted acid ion liquid to preparation of diphenyl oxalate |
-
2002
- 2002-08-28 CN CNB021292132A patent/CN1164558C/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CN1412176A (en) | 2003-04-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1950321A (en) | Process for preparing carboxylic acids and derivatives thereof | |
| CN1597096A (en) | Catalyst used for synthesizing dimethyl carbonate from ured and methanol and its preparation method and application | |
| CN1034531A (en) | The method of dehydrogenating of cyclonene | |
| CN1687003A (en) | Method for synthesizing phenyloxalate from dicthyl oxalate and phenol | |
| CN1723187A (en) | Continuous method for preparing ethyl lactate | |
| CN1631886A (en) | Process for synthesizing cyclic carbonic ester | |
| CN114656345B (en) | Synthesis method of 4-methyl-1-pentene | |
| CN1164558C (en) | Method for preparing methyl phenyl oxalate and phenostal | |
| CN101033177A (en) | Method of synthesizing 2-ethoxy-phenol | |
| CN1167664C (en) | Catalytic synthesis of methyl phenyl oxalate and phenostal by using load metal oxide | |
| CN101961650B (en) | Zirconium base catalyst, preparation method and application in preparation of anhydrous formaldehyde | |
| CN1164559C (en) | Preparation method of methyl phenyl oxalate and phenostal | |
| CN1078876C (en) | Process for production of alkyl ether of phenol and catalyst used therein | |
| CN1255210C (en) | Preparing method for loaded titania catalyst of ester interchange synthetic phenyl ester oxalate | |
| CN100420667C (en) | Methyl phenyl oxalate and diphenyl oxalate synthesizing process catalyzed with composite carrier supported metal oxide | |
| CN1268422C (en) | Preparation of loaded molybdenum oxide catalyst for synthesis of phenyloxalate by ester interchange process | |
| CN1224454C (en) | Catalyst for direct synthesis of methyl carbonate and its prepn | |
| CN1868992A (en) | Alkylphenol coproduction technology | |
| CN1317268C (en) | 2,6-dimethylpyridine preparation method | |
| CN1199934C (en) | Urea alcoholizing process of synthesizing dimethyl carbonate | |
| CN1583708A (en) | Catalytic synthesis of phenyloxalate and methyl phenyl oxalate | |
| CN101544553B (en) | Method for synthesizing cyclohexanone dimer by continuous catalytic reaction and distillation | |
| CN1562952A (en) | Method for catalyzer synthesizing methyl-phenyl-oxalate and phenostal | |
| CN1120049C (en) | Supported type heteropolya cid catalyst in synthesis of ethylene glycol series monoethers acetate | |
| CN1562953A (en) | method for synthesizing methyl phenyl oxalate and phenostal under catalysis of oxide of bimetal |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term |
Granted publication date: 20040901 |
|
| CX01 | Expiry of patent term |